Data from: Lack of evidence for selection favouring MHC haplotypes that combine high functional diversity
收藏DataONE2017-12-15 更新2024-06-26 收录
下载链接:
https://search.dataone.org/view/null
下载链接
链接失效反馈官方服务:
资源简介:
High rates of gene duplication and the highest levels of functional allelic diversity in vertebrate genomes are the main hallmarks of the major histocompatibility complex (MHC), a multigene family with a primordial role in pathogen recognition. The usual tight linkage among MHC gene duplicates may provide an opportunity for the evolution of haplotypes that associate functionally divergent alleles and thus grant the transmission of optimal levels of diversity to coming generations. Even though such associations may be a crucial component of disease resistance, this hypothesis has been given little attention in wild populations. Here, we leveraged pedigree data from a barn owl (Tyto alba) population to characterize MHC haplotype structure across two MHC class I (MHC-I) and two MHC class IIB (MHC-IIB) duplicates, in order to test the hypothesis that haplotypes’ genetic diversity is higher than expected from randomly associated alleles. After showing that MHC loci are tightly linked within classes, we found limited evidence for shifts towards MHC haplotypes combining high diversity. Neither amino acid nor functional within-haplotype diversity were significantly higher than in random sets of haplotypes, regardless of MHC class. Our results therefore provide no evidence for selection towards high-diversity MHC haplotypes in barn owls. Rather, high rates of convergent evolution may constrain the evolution of high-diversity haplotypes at MHC-I, while, in contrast, for MHC-IIB, fixed differences among loci may provide barn owls with already optimized functional diversity. This suggests that at the MHC-I and MHC-IIB, respectively, different evolutionary dynamics may govern the evolution of within-haplotype diversity.
脊椎动物基因组中,高基因重复率与最高水平的功能等位基因多样性,是主要组织相容性复合体 (major histocompatibility complex, MHC) 的核心标志性特征;该多基因家族在病原体识别中发挥着原始演化作用。MHC基因重复拷贝间普遍存在的紧密连锁,或许为单倍型的演化提供了契机:这类单倍型可结合功能分化的等位基因,从而将最优水平的多样性传递给后代。尽管这类等位基因关联或许是疾病抗性的关键组成部分,但该假说在野生种群中尚未得到充分关注。本研究利用仓鸮 (Tyto alba) 种群的谱系数据,对2个MHC I类 (MHC class I, MHC-I) 与2个MHC IIB类 (MHC class IIB, MHC-IIB) 基因重复拷贝的单倍型结构进行解析,以检验"单倍型遗传多样性高于随机关联等位基因预期水平"这一假说。在证实MHC基因座在同一类别内紧密连锁后,我们仅发现有限证据支持向高多样性MHC单倍型的演化趋势。无论MHC类别如何,单倍型内的氨基酸多样性与功能多样性均未显著高于随机组合的单倍型集。因此,本研究结果未发现仓鸮存在针对高多样性MHC单倍型的选择作用。与之相反,MHC-I区域高频率的趋同演化或许会限制高多样性单倍型的演化;而对于MHC-IIB而言,基因座间的固定差异或许已为仓鸮提供了最优的功能多样性。这表明,MHC-I与MHC-IIB区域的单倍型内多样性演化,分别受不同的演化动力所调控。
创建时间:
2017-12-15



